Allele Registry

Canonical Allele Identifier: PA266750

Gene: SLC25A13 HGNC NCBI

ClinVar Allele:

97542

ClinVar RCV:

RCV000077782

RCV000292034

RCV000404137

RCV001854367

RCV003474671

ClinVar Variation:

92110

HGVS (amino-acid)	Matching Registered Transcripts
NP_055066.1:p.Arg355Gln	CA266749 NM_014251.3:c.1064G>A