Canonical Allele Identifier: PA2499255909
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 1209788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365173.1:p.Arg52His
CA6909569
NM_001378244.1:c.155G>A