Allele Registry

Canonical Allele Identifier: PA2825095998

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000211579

ClinVar Variation:

226415

HGVS (amino-acid)	Matching Registered Transcripts
NP_000222.2:p.Ser230Arg	CA10576342 NM_000231.3:c.690T>A CA387502913 NM_000231.3:c.688A>C CA387502925 NM_000231.3:c.690T>G