Canonical Allele Identifier: PA159533
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 134334
ClinVar RCV Id: RCV000121008 RCV000229853 RCV003884352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg89Leu
CA159531
NM_021922.3:c.266G>T