Canonical Allele Identifier: PA2573101655
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 424470
ClinVar RCV Id: RCV000482550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996816.3:p.Cys795Tyr
CA1396239
NM_206933.4:c.2384G>A