Canonical Allele Identifier: PA178064
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 165320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Arg1073Gln
CA178063
NM_153700.2:c.3218G>A