Canonical Allele Identifier: PA1139754333
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 964253
ClinVar RCV Id: RCV001238441 RCV001819936 RCV002491774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu111Pro
CA5924369
NM_022725.4:c.332T>C