Canonical Allele Identifier: PA2828751535
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 2006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Cys283Tyr
CA339932
NM_001378246.1:c.848G>A