Canonical Allele Identifier: PA915977465
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg34His
CA199071
NM_001135697.3:c.101G>A