Canonical Allele Identifier: PA2499289394
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1037435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln219Arg
CA380058601
NM_022725.4:c.656A>G