Canonical Allele Identifier: PA916068460
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 662729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Met163Ile
CA380058940
NM_022725.4:c.489G>T
CA380058941
NM_022725.4:c.489G>C
CA380058942
NM_022725.4:c.489G>A