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ALS1
TP53
Amyotrophic Lateral Sclerosis 1
Lynch Syndrome
Cystic Fibrosis
COL4A5
Cowden Syndrome 1
Trp53
Dilated Cardiomyopathy
Phenylketonuria
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Variant Search
Amino acid Coordinates:--
AA:--
Codon:--
Clinvar ID
Nucleotide
Protein
Type
Clinical Significance
Homo Sapiens
SCN2A Variant
Genomic mutations
Protein mutations
Clear
SCN2A Sequence
All
P: 0
LP: 0
LB: 0
B: 0
VUS: 0
#: mutation count; +: mutation count ≥ 99.
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Comparison
Al agent
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