Canonical Allele Identifier: PA915977543
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg81Cys
CA220233
NM_001135697.3:c.241C>T