Canonical Allele Identifier: PA2829689196
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1424569
ClinVar RCV Id: RCV001957205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gly743Ala
CA344865515
NM_007123.6:c.2228G>C