Canonical Allele Identifier: PA2573283405
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1406386
ClinVar RCV Id: RCV001906892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gln290Pro
CA380058164
NM_022725.4:c.869A>C