Canonical Allele Identifier: PA891866034
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 30703
ClinVar RCV Id: RCV000023681 RCV000169775 RCV000987440 RCV001047050 RCV001356848 RCV002276570 RCV003324499 RCV004532400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Leu550Ser
CA199262
NM_001317924.2:c.1649T>C