Allele Registry

Canonical Allele Identifier: PA207763

Gene: SDCCAG8 HGNC NCBI

ClinVar Allele:

206784

ClinVar RCV:

RCV000193940

RCV000873932

RCV001558681

RCV004541252

ClinVar Variation:

212138

HGVS (amino-acid)	Matching Registered Transcripts
NP_006633.1:p.Asp501His	CA207762 NM_006642.5:c.1501G>C