Canonical Allele Identifier: PA2829689750
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1800581
ClinVar RCV Id: RCV002461720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Pro1058Thr
CA344862617
NM_007123.6:c.3172C>A