Canonical Allele Identifier: PA2826972806
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 191190
ClinVar RCV Id: RCV000171376 RCV002515238 RCV003989482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Ser766Ile
CA236213
NM_001317924.2:c.2297G>T