Canonical Allele Identifier: PA2828751426
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 530807
ClinVar RCV Id: RCV000636846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Arg166Gln
CA6909702
NM_001378246.1:c.497G>A