Allele Registry

Canonical Allele Identifier: PA2825383374

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004100945

ClinVar Variation:

2238725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034444.1:p.Ala298Val	CA390971782 NM_001039355.3:c.893C>T