Canonical Allele Identifier: PA645431650
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 304209
ClinVar RCV Id: RCV000272674 RCV002522195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Met1Thr