Canonical Allele Identifier: PA2829687947
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 143182
ClinVar RCV Id: RCV000132713 RCV001075672 RCV001227152 RCV003453101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Val164Phe
CA270157
NM_007123.6:c.490G>T