Canonical Allele Identifier: PA658661882
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 471924
ClinVar RCV Id: RCV000537323 RCV001797103 RCV001821581 RCV002530181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg69Gln
CA3771352
NM_021922.3:c.206G>A