Canonical Allele Identifier: PA645431648
Gene: FANCF HGNC NCBI
ClinVar Allele:
398569
ClinVar RCV:
RCV000462200
ClinVar Variation:
408144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Met1Arg