Canonical Allele Identifier: PA2829689362
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1519126
ClinVar RCV Id: RCV002024374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Arg837Trp
CA1396220
NM_007123.6:c.2509C>T