Canonical Allele Identifier: PA1139754355
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 992566
ClinVar RCV Id: RCV001281065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Gly118Val
CA219086646
NM_022725.4:c.353G>T