Canonical Allele Identifier: PA2573095356
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1319635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.His267Gln
CA5924257
NM_022725.4:c.801C>G
CA5924258
NM_022725.4:c.801C>A