Canonical Allele Identifier: PA091241
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 286049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Glu137Lys
CA501039
NM_000023.3:c.409G>A