Canonical Allele Identifier: PA2829690272
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1412641
ClinVar RCV Id: RCV001923354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Ala1351Val
CA1395843
NM_007123.6:c.4052C>T