Allele Registry

Canonical Allele Identifier: PA2580210046

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004088391

ClinVar Variation:

2223554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339750.1:p.Gly274Glu	CA7344229 NM_001352821.2:c.821G>A