Canonical Allele Identifier: PA2829689846
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 242397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Tyr1123Cys
CA1396001
NM_007123.6:c.3368A>G