Canonical Allele Identifier: PA915977433
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 538663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Gly17Arg
CA8643683
NM_001135697.3:c.49G>A
CA400176330
NM_001135697.3:c.49G>C