Canonical Allele Identifier: PA645431691
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 304203
ClinVar RCV Id: RCV000285884 RCV001850617 RCV003488515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Leu146Val
CA5924331
NM_022725.4:c.436C>G