Canonical Allele Identifier: PA2829988439
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 539293
ClinVar RCV Id: RCV000648999 RCV002257904 RCV002235507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Pro536_Ter537insLeuProSerThrLysGlyProProSerTrpCysSerIleThrSerPheLeuLysGlyIleSerPhePheThrThrLeuSer
CA3771765
NM_021922.3:c.1610G>T