Canonical Allele Identifier: PA2826972562
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 127155
ClinVar RCV Id: RCV000115011 RCV001281114 RCV001753491 RCV001854543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Asp333His
CA151406
NM_001317924.2:c.997G>C