Canonical Allele Identifier: PA2741982776
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2708853
ClinVar RCV Id: RCV003524208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ala257Thr
CA380058363
NM_022725.4:c.769G>A