Canonical Allele Identifier: PA2825095891
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 530807
ClinVar RCV Id: RCV000636846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000222.2:p.Arg166Gln
CA6909702
NM_000231.3:c.497G>A