Canonical Allele Identifier: PA2827243857
Gene: WDR59 HGNC NCBI

Linked Data

ClinVar Variation Id: 2474425
ClinVar RCV Id: RCV004266731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311100.1:p.Pro517Ser
CA8171204
NM_001324171.2:c.1549C>T