Canonical Allele Identifier: PA2580456721
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2100607
ClinVar RCV Id: RCV003033543
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln130Glu
CA380059148
NM_022725.4:c.388C>G