Home
Tools
About RDDC
Contact Us
ALS1
TP53
Amyotrophic Lateral Sclerosis 1
Lynch Syndrome
Cystic Fibrosis
COL4A5
Cowden Syndrome 1
Trp53
Dilated Cardiomyopathy
Phenylketonuria
中文
EN
Amino acid Coordinates:--
AA:--
Codon:--
Clinvar ID
Codon
Nucleotide
Protein
Type
Clinical Significance
AI Predictor
Homo Sapiens
PDE6H Variant
Genomic mutations
Protein mutations
Search
?
PDE6H Sequence
All
P: 0
LP: 0
LB: 0
B: 0
VUS: 0
Variant of Interest
Wechat
Comparison
Al agent
Back to top