Canonical Allele Identifier: PA645429041
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 356444
ClinVar RCV Id: RCV000467424 RCV001269487 RCV001653707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Pro85Ser
CA3771366
NM_021922.3:c.253C>T