Canonical Allele Identifier: PA093035
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 30703
ClinVar RCV Id: RCV000023681 RCV000169775 RCV000987440 RCV001047050 RCV001356848 RCV002276570 RCV003324499 RCV004532400
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Leu710Ser
CA199262
NM_025132.4:c.2129T>C