Canonical Allele Identifier: PA2580456747
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2156899
ClinVar RCV Id: RCV003091031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu169Gln
CA219086640
NM_022725.4:c.506T>A