Canonical Allele Identifier: PA159524
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 134331
ClinVar RCV Id: RCV000121005 RCV000687310 RCV002257437 RCV003237728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Pro18Ser
CA159522
NM_021922.3:c.52C>T