Canonical Allele Identifier: PA915977632
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 188733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Ile124Thr
CA199048
NM_001135697.3:c.371T>C