Canonical Allele Identifier: PA658665528
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 452720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg221Cys
CA8643859
NM_000023.3:c.661C>T