Canonical Allele Identifier: PA645439103
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 288595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg181Ser
CA8643819
NM_000023.3:c.541C>A