Allele Registry

Canonical Allele Identifier: PA2828751489

Gene: SGCG HGNC NCBI

ClinVar Variation Id: 226415

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365175.1:p.Ser230Arg	CA10576342 NM_001378246.1:c.690T>A CA387502913 NM_001378246.1:c.688A>C CA387502925 NM_001378246.1:c.690T>G