Canonical Allele Identifier: PA916068450
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 701972
ClinVar RCV Id: RCV000870754 RCV001817000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Arg138Ser
CA5924339
NM_022725.4:c.412C>A