Canonical Allele Identifier: PA2580431290
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2004950
ClinVar RCV Id: RCV002828406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Pro181Ser
CA363773117
NM_021922.3:c.541C>T