Allele Registry

Canonical Allele Identifier: PA159586

Gene: FANCF HGNC NCBI

ClinVar Allele:

138094

ClinVar RCV:

RCV000121029

RCV000457324

ClinVar Variation:

134355

HGVS (amino-acid)	Matching Registered Transcripts
NP_073562.1:p.Gly243Glu	CA159584 NM_022725.4:c.728G>A