Allele Registry

Canonical Allele Identifier: PA645431703

Gene: FANCF HGNC NCBI

ClinVar Variation Id: 304201

HGVS (amino-acid)	Matching Registered Transcripts
NP_073562.1:p.Tyr287Cys	CA5924242 NM_022725.4:c.860A>G