Canonical Allele Identifier: PA645501785
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_079408.3:p.Arg1223Cys
CA2892440
NM_025132.4:c.3667C>T