Allele Registry

Canonical Allele Identifier: PA2499234895

Gene: FBXO47 HGNC NCBI

ClinVar RCV:

RCV001649519

ClinVar Variation:

1247558

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008777.2:p.Gln209Arg	CA8527230 NM_001008777.3:c.626A>G