Allele Registry

Canonical Allele Identifier: PA2825383363

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004088391

ClinVar Variation:

2223554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034444.1:p.Gly221Glu	CA7344229 NM_001039355.3:c.662G>A