Allele Registry

Canonical Allele Identifier: PA2825095747

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000366203

RCV001850454

ClinVar Variation:

289650

HGVS (amino-acid)	Matching Registered Transcripts
NP_000222.2:p.Leu53Pro	CA10606508 NM_000231.3:c.158T>C