Canonical Allele Identifier: PA645439073
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 283227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg98Pro
CA10604429
NM_000023.3:c.293G>C