Allele Registry

Canonical Allele Identifier: PA106002

Gene: SLC25A4 HGNC NCBI

ClinVar RCV:

RCV000019908

ClinVar Variation:

18246

HGVS (amino-acid)	Matching Registered Transcripts
NP_001142.2:p.Val289Met	CA127985 NM_001151.4:c.865G>A