Canonical Allele Identifier: PA645431693
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 408146
ClinVar RCV Id: RCV000462923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu157Phe
CA16613287
NM_022725.4:c.469C>T