Canonical Allele Identifier: PA916068503
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 659459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Pro213Ser
CA5924294
NM_022725.4:c.637C>T