Canonical Allele Identifier: PA916022112
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 437272
ClinVar RCV Id: RCV000500098 RCV000951959 RCV001532019 RCV001149215 RCV001149216 RCV004541573 RCV002279282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304853.1:p.Glu843Gly
CA2892240
NM_001317924.2:c.2528A>G