Canonical Allele Identifier: PA2828751197
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 499009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Leu192Arg
CA387504403
NM_001378245.1:c.575T>G