Allele Registry

Canonical Allele Identifier: PA2827683111

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004088391

ClinVar Variation:

2223554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339749.1:p.Gly155Glu	CA7344229 NM_001352820.2:c.464G>A