Canonical Allele Identifier: PA658812245
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 505196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.Trp1734Arg
CA7527782
NM_153700.2:c.5200T>C
CA392158152
NM_153700.2:c.5200T>A