Allele Registry

Canonical Allele Identifier: PA2826808672

Gene: SLC25A29 HGNC NCBI

ClinVar RCV:

RCV004088391

ClinVar Variation:

2223554

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278742.1:p.Gly155Glu	CA7344229 NM_001291813.2:c.464G>A