Allele Registry

Canonical Allele Identifier: PA105986

Gene: SLC25A4 HGNC NCBI

ClinVar RCV:

RCV000019909

ClinVar Variation:

18247

HGVS (amino-acid)	Matching Registered Transcripts
NP_001142.2:p.Leu98Pro	CA127986 NM_001151.4:c.293T>C