Canonical Allele Identifier: PA915977495
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 290930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Ala64Thr
CA8643731
NM_001135697.3:c.190G>A