Canonical Allele Identifier: PA2573278451
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1499186
ClinVar RCV Id: RCV002010482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Lys231del
CA1620905595
NM_021922.3:c.691_693del