Canonical Allele Identifier: PA2573283365
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1390601
ClinVar RCV Id: RCV001910781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Ile205Thr
CA5924301
NM_022725.4:c.614T>C