Canonical Allele Identifier: PA2829625019
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 1003465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005700.2:p.Gly168Ser
CA218461363
NM_005709.4:c.502G>A