Canonical Allele Identifier: PA2829689679
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 166513
ClinVar RCV Id: RCV000152628 RCV000477797 RCV001034259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.His1015Tyr
CA179580
NM_007123.6:c.3043C>T