Allele Registry

Canonical Allele Identifier: PA2827936295

Gene: SLC25A38 HGNC NCBI

ClinVar Allele:

290284

ClinVar RCV:

RCV000278029

RCV000330775

RCV000425850

RCV000968454

RCV002523257

ClinVar Variation:

345145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341727.1:p.Thr80Arg	CA2327393 NM_001354798.2:c.239C>G