Canonical Allele Identifier: PA2825096037
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 2009
ClinVar RCV Id: RCV000002086 RCV000078408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000222.2:p.Glu263Lys
CA220515
NM_000231.3:c.787G>A