Canonical Allele Identifier: PA261117
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 39427
ClinVar RCV Id: RCV000032622 RCV000662094 RCV000662095 RCV000675046 RCV001377937
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005700.2:p.Arg103His
CA261116
NM_005709.4:c.308G>A