Allele Registry

Canonical Allele Identifier: PA2826537723

Gene: FBXO38 HGNC NCBI

ClinVar Allele:

1005949

ClinVar RCV:

RCV002241917

ClinVar Variation:

1014068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258652.1:p.Ser592Ala	CA361655358 NM_001271723.2:c.1774T>G