Canonical Allele Identifier: PA2829689290
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1508017
ClinVar RCV Id: RCV002013737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Asp798Gly
CA344864889
NM_007123.6:c.2393A>G