Allele Registry

Canonical Allele Identifier: PA2830297910

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004100945

ClinVar Variation:

2238725

HGVS (amino-acid)	Matching Registered Transcripts
NP_689546.1:p.Ala232Val	CA390971782 NM_152333.3:c.695C>T