Canonical Allele Identifier: PA2573095355
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1337361
ClinVar RCV Id: RCV001820375 RCV002542615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu262Ser
CA5924262
NM_022725.4:c.785T>C