Canonical Allele Identifier: PA645501756
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 437272
ClinVar RCV Id: RCV000500098 RCV000951959 RCV001532019 RCV001149215 RCV001149216 RCV004541573 RCV002279282
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Glu1003Gly
CA2892240
NM_025132.4:c.3008A>G