Canonical Allele Identifier: PA2499289389
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 998327
ClinVar RCV Id: RCV001294130 RCV003166632 RCV001859242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Tyr151Phe
CA5924328
NM_022725.4:c.452A>T