Allele Registry

Canonical Allele Identifier: PA2826171276

Gene: SLC25A22 HGNC NCBI

ClinVar Allele:

202642

ClinVar RCV:

RCV000189308

RCV002514062

ClinVar Variation:

207149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177989.1:p.Val45Met	CA318335 NM_001191060.2:c.133G>A