Canonical Allele Identifier: PA2829689457
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1356073
ClinVar RCV Id: RCV001876647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Met899Leu
CA1396187
NM_007123.6:c.2695A>C
CA344864235
NM_007123.6:c.2695A>T