Canonical Allele Identifier: PA915977526
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 188811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg74Trp
CA199069
NM_001135697.3:c.220C>T