Canonical Allele Identifier: PA915977469
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 217250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg34Cys
CA210084
NM_001135697.3:c.100C>T