Allele Registry

Canonical Allele Identifier: PA645431660

Gene: FANCF HGNC NCBI

ClinVar RCV:

RCV000225823

RCV000764969

RCV001820762

RCV003492014

RCV003884425

ClinVar Variation:

241437

HGVS (amino-acid)	Matching Registered Transcripts
NP_073562.1:p.Ala81Ser	CA5924392 NM_022725.4:c.241G>T