Canonical Allele Identifier: PA915977440
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 254720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Thr21Ile
CA8643686
NM_001135697.3:c.62C>T