Canonical Allele Identifier: PA645501699
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 424472
ClinVar RCV Id: RCV000479045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Leu206Pro
CA16618044
NM_025132.4:c.617T>C