Canonical Allele Identifier: PA1139754436
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 878062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.His227Arg
CA380058548
NM_022725.4:c.680A>G