Canonical Allele Identifier: PA2830054146
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2068704
ClinVar RCV Id: RCV002975029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Leu211Val
CA356633803
NM_025132.4:c.631T>G