Canonical Allele Identifier: PA2573095030
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1327104
ClinVar RCV Id: RCV001788984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg221Gln
CA3771462
NM_021922.3:c.662G>A