Canonical Allele Identifier: PA645501751
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 286674
ClinVar RCV Id: RCV000391331 RCV000756917 RCV001089411 RCV002519250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.His891Tyr
CA2892155
NM_025132.4:c.2671C>T