Canonical Allele Identifier: PA2829625973
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 2157092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005700.2:p.Met449Thr
CA5904263
NM_005709.4:c.1346T>C