Canonical Allele Identifier: PA2829689301
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 156393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Gly805Ala
CA270788
NM_007123.6:c.2414G>C