Canonical Allele Identifier: PA182566
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 178563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005700.2:p.Ala504Thr
CA182565
NM_005709.4:c.1510G>A