Canonical Allele Identifier: PA2573316369
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1375709
ClinVar RCV Id: RCV001883417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Tyr3143Cys
CA344825192
NM_206933.4:c.9428A>G