Canonical Allele Identifier: PA2741982785
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2891400
ClinVar RCV Id: RCV003636459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.His286Pro
CA5924245
NM_022725.4:c.857A>C