Canonical Allele Identifier: PA185525
Gene: USH1C HGNC NCBI

Linked Data

ClinVar Variation Id: 179964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_710142.1:p.Pro608Ser
CA185524
NM_153676.4:c.1822C>T