Canonical Allele Identifier: PA2829689917
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 424938
ClinVar RCV Id: RCV000488016 RCV001199794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009054.6:p.Leu1154Ser
CA16621593
NM_007123.6:c.3461T>C