Allele Registry

Canonical Allele Identifier: PA2826537722

Gene: FBXO38 HGNC NCBI

ClinVar RCV:

RCV001520003

RCV001655777

RCV002241363

ClinVar Variation:

1169150

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258652.1:p.Ser592Pro	CA3497380 NM_001271723.2:c.1774T>C