Canonical Allele Identifier: PA2573278417
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1404192
ClinVar RCV Id: RCV001898956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Leu178Trp
CA3771432
NM_021922.3:c.533T>G