Allele Registry

Canonical Allele Identifier: PA2499282672

Gene: CENPF HGNC NCBI

ClinVar RCV:

RCV001578860

RCV001673217

ClinVar Variation:

1209683

HGVS (amino-acid)	Matching Registered Transcripts
NP_057427.3:p.Arg2943Gly	CA1391504 NM_016343.4:c.8827A>G