Canonical Allele Identifier: PA178052
Gene: STRC HGNC NCBI

Linked Data

ClinVar Variation Id: 165312
ClinVar RCV Id: RCV000151951 RCV002467598
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714544.1:p.His1298Arg
CA178051
NM_153700.2:c.3893A>G