Canonical Allele Identifier: PA916060694
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 652052
ClinVar RCV Id: RCV000807538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg219Ile
CA3771459
NM_021922.3:c.656G>T