Canonical Allele Identifier: PA2580456722
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2303644
ClinVar RCV Id: RCV002879018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln130Arg
CA5924347
NM_022725.4:c.389A>G