Canonical Allele Identifier: PA2829689256
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 178583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asp778Tyr
CA182608
NM_007123.6:c.2332G>T