Canonical Allele Identifier: PA2828751493
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 448361
ClinVar Variation Id: 1400512
ClinVar RCV Id: RCV001932746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365175.1:p.Val236Met
CA6909833
NM_001378246.1:c.706G>A
CA2573149098
NM_001378246.1:c.705_706delinsCA