Allele Registry

Canonical Allele Identifier: PA2828751326

Gene: SGCG HGNC NCBI

ClinVar RCV:

RCV000366203

RCV001850454

ClinVar Variation:

289650

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365175.1:p.Leu53Pro	CA10606508 NM_001378246.1:c.158T>C