Canonical Allele Identifier: PA261118
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 39427
ClinVar RCV Id: RCV000032622 RCV000662094 RCV000662095 RCV000675046 RCV001377937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_710142.1:p.Arg103His
CA261116
NM_153676.4:c.308G>A