Canonical Allele Identifier: PA2573283346
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1433197
ClinVar RCV Id: RCV001982194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Arg135Leu
CA5924343
NM_022725.4:c.404G>T