Canonical Allele Identifier: PA891851519
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 565869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ser265Arg
CA5924260
NM_022725.4:c.795C>A
CA380058311
NM_022725.4:c.795C>G
CA380058317
NM_022725.4:c.793A>C