Canonical Allele Identifier: PA2826972923
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 348754
ClinVar RCV Id: RCV000288576 RCV000385239 RCV001083150 RCV004530412 RCV000488404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Arg1063Cys
CA2892440
NM_001317924.2:c.3187C>T