Canonical Allele Identifier: PA2573283330
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1464426
ClinVar RCV Id: RCV001975450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Tyr109His
CA380059270
NM_022725.4:c.325T>C