Canonical Allele Identifier: PA2580456710
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1937599
ClinVar RCV Id: RCV002642862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gly118Ser
CA380059217
NM_022725.4:c.352G>A