Canonical Allele Identifier: PA2499288443
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1044189
ClinVar RCV Id: RCV001348403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.His229Tyr
CA3771464
NM_021922.3:c.685C>T