Canonical Allele Identifier: PA2829690119
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 940553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ala1267Val
CA1395920
NM_007123.6:c.3800C>T