Canonical Allele Identifier: PA658825302
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 554420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Glu137Gln
CA400179814
NM_000023.3:c.409G>C