Canonical Allele Identifier: PA915977565
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 283227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg98Pro
CA10604429
NM_001135697.3:c.293G>C