Canonical Allele Identifier: PA2828751275
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 285833
ClinVar RCV Id: RCV000309697 RCV000338071 RCV000399428 RCV001094189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Gly278Ser
CA6909860
NM_001378245.1:c.832G>A