Allele Registry

Canonical Allele Identifier: PA2830057832

Gene: FBXO38 HGNC NCBI

ClinVar Allele:

1005949

ClinVar RCV:

RCV002241917

ClinVar Variation:

1014068

HGVS (amino-acid)	Matching Registered Transcripts
NP_110420.3:p.Ser592Ala	CA361655358 NM_030793.5:c.1774T>G