Canonical Allele Identifier: PA2573315701
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1390049
ClinVar RCV Id: RCV001917501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Cys792Tyr
CA344864933
NM_206933.4:c.2375G>A