Canonical Allele Identifier: PA645439048
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 290930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Ala64Thr
CA8643731
NM_000023.3:c.190G>A