Canonical Allele Identifier: PA2827243879
Gene: WDR59 HGNC NCBI

Linked Data

ClinVar Variation Id: 785540
ClinVar RCV Id: RCV000967422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311101.1:p.Pro274Ala
CA8171498
NM_001324172.2:c.820C>G