Canonical Allele Identifier: PA658661859
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 456284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ser191Arg
CA5924307
NM_022725.4:c.573C>A
CA5924308
NM_022725.4:c.573C>G
CA380058772
NM_022725.4:c.571A>C