Allele Registry

Canonical Allele Identifier: PA2826808702

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004100945

ClinVar Variation:

2238725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278743.1:p.Ala232Val	CA390971782 NM_001291814.2:c.695C>T