Allele Registry

Canonical Allele Identifier: PA2580210066

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004100945

ClinVar Variation:

2238725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339750.1:p.Ala351Val	CA390971782 NM_001352821.2:c.1052C>T