Canonical Allele Identifier: PA2829690237
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1369459
ClinVar RCV Id: RCV001894906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Lys1334Arg
CA1395856
NM_007123.6:c.4001A>G