Canonical Allele Identifier: PA159537
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 134336
ClinVar RCV Id: RCV000121010 RCV000689014 RCV003153392 RCV003389394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Pro310Gln
CA159535
NM_021922.3:c.929C>A