Allele Registry

Canonical Allele Identifier: PA913192706

Gene: SLC25A13 HGNC NCBI

ClinVar Variation Id: 594933

HGVS (amino-acid)	Matching Registered Transcripts
NP_055066.1:p.Arg292Trp	CA4353113 NM_014251.3:c.874C>T