Canonical Allele Identifier: PA2580456777
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2191808
ClinVar RCV Id: RCV002620790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.His267Tyr
CA380058304
NM_022725.4:c.799C>T