Canonical Allele Identifier: PA2825096003
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 448361
ClinVar RCV Id: RCV000518177 RCV001829477
ClinVar Variation Id: 1400512
ClinVar RCV Id: RCV001932746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000222.2:p.Val236Met
CA6909833
NM_000231.3:c.706G>A
CA2573149098
NM_000231.3:c.705_706delinsCA