Canonical Allele Identifier: PA159568
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 134348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu129Val
CA159566
NM_022725.4:c.385C>G