Canonical Allele Identifier: PA645431684
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 408145
ClinVar RCV Id: RCV000468810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Pro119Leu
CA5924361
NM_022725.4:c.356C>T