Canonical Allele Identifier: PA2826972459
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2147128
ClinVar RCV Id: RCV003077030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Arg112His
CA2891711
NM_001317924.2:c.335G>A