Canonical Allele Identifier: PA645431700
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 252737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln211His
CA5924296
NM_022725.4:c.633G>T
CA380058640
NM_022725.4:c.633G>C