Allele Registry

Canonical Allele Identifier: PA645431672

Gene: FANCF HGNC NCBI

ClinVar RCV:

RCV000229804

RCV001820763

RCV003153540

RCV003316303

RCV003955369

ClinVar Variation:

241438

HGVS (amino-acid)	Matching Registered Transcripts
NP_073562.1:p.Pro117Thr	CA5924364 NM_022725.4:c.349C>A