Canonical Allele Identifier: PA2825095939
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 499009
ClinVar RCV Id: RCV000592624 RCV001347465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000222.2:p.Leu192Arg
CA387504403
NM_000231.3:c.575T>G