Allele Registry

Canonical Allele Identifier: PA2826171287

Gene: SLC25A22 HGNC NCBI

ClinVar Allele:

142834

ClinVar RCV:

RCV000147503

RCV000178365

RCV000472638

RCV001507783

RCV002316411

RCV003915274

ClinVar Variation:

139131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177989.1:p.Asp51Asn	CA173468 NM_001191060.2:c.151G>A