Canonical Allele Identifier: PA2573278353
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1351105
ClinVar RCV Id: RCV002042367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg89Pro
CA363772368
NM_021922.3:c.266G>C