Canonical Allele Identifier: PA2573283342
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1436499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ala124Ser
CA380059187
NM_022725.4:c.370G>T