Canonical Allele Identifier: PA2741982753
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2815148
ClinVar RCV Id: RCV003637126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Glu131Lys
CA380059143
NM_022725.4:c.391G>A