Canonical Allele Identifier: PA2741982751
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2739326
ClinVar RCV Id: RCV003523492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu129Ile
CA380059152
NM_022725.4:c.385C>A