Allele Registry

Canonical Allele Identifier: PA318389

Gene: SLC25A22 HGNC NCBI

ClinVar RCV:

RCV000636275

RCV000678848

RCV001721220

RCV002314763

ClinVar Variation:

207170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177990.1:p.Val227Met	CA318388 NM_001191061.2:c.679G>A