Canonical Allele Identifier: PA2827243828
Gene: WDR59 HGNC NCBI

Linked Data

ClinVar Variation Id: 2541958
ClinVar RCV Id: RCV004314060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311100.1:p.Ala19Val
CA396848231
NM_001324171.2:c.56C>T