Canonical Allele Identifier: PA2573198559
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1445005
ClinVar RCV Id: RCV001982689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Ala63Thr
CA356633951
NM_001317924.2:c.187G>A