Allele Registry

Canonical Allele Identifier: PA658830690

Gene: FBXO11 HGNC NCBI

ClinVar RCV:

RCV000677378

RCV001291313

ClinVar Variation:

559601

HGVS (amino-acid)	Matching Registered Transcripts
NP_079409.3:p.Arg54Ser	CA346813373 NM_025133.4:c.162A>C CA346813374 NM_025133.4:c.162A>T