Canonical Allele Identifier: PA1139754455
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 957563
ClinVar RCV Id: RCV001230558
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Arg266Cys
CA5924259
NM_022725.4:c.796C>T