Canonical Allele Identifier: PA2573283348
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1373268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Arg140Gln
CA219086645
NM_022725.4:c.419G>A