Canonical Allele Identifier: PA1139751055
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 992076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_710142.1:p.Arg754Trp
CA5904260
NM_153676.4:c.2260C>T