Canonical Allele Identifier: PA2829689390
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1713573
ClinVar RCV Id: RCV002302968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Lys863Arg
CA1396205
NM_007123.6:c.2588A>G