Allele Registry

Canonical Allele Identifier: PA2826171280

Gene: SLC25A22 HGNC NCBI

ClinVar Allele:

202641

ClinVar RCV:

RCV000727499

RCV001080737

RCV002054230

RCV002390499

ClinVar Variation:

207161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177989.1:p.Thr47Met	CA318363 NM_001191060.2:c.140C>T