Canonical Allele Identifier: PA2825096040
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 2063856
ClinVar RCV Id: RCV002943016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000222.2:p.Cys267Ser
CA6909849
NM_000231.3:c.800G>C
CA387503815
NM_000231.3:c.799T>A
CA658832944
NM_000231.3:c.[800G>C;801T>C]
CA2580086817
NM_000231.3:c.800_801delinsCC