Canonical Allele Identifier: PA916056584
Gene: WDR59 HGNC NCBI

Linked Data

ClinVar Variation Id: 785539
ClinVar RCV Id: RCV000967421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085058.3:p.Gly803Cys
CA8170827
NM_030581.4:c.2407G>T