Canonical Allele Identifier: PA1139745683
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 939255
ClinVar RCV Id: RCV001208626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Gly174Val
CA363773079
NM_021922.3:c.521G>T