Canonical Allele Identifier: PA2829689438
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 550419
ClinVar RCV Id: RCV001075434 RCV001098933 RCV001376385 RCV001244238 RCV001731856 RCV000778220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.His885Tyr
CA1396195
NM_007123.6:c.2653C>T