Canonical Allele Identifier: PA2580471671
Gene: WDR59 HGNC NCBI

Linked Data

ClinVar Variation Id: 2326230
ClinVar RCV Id: RCV004165632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085058.3:p.Glu498Lys
CA396780245
NM_030581.4:c.1492G>A