Canonical Allele Identifier: PA2573287360
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494663
ClinVar RCV Id: RCV001989515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Gly866Asp
CA356638483
NM_025132.4:c.2597G>A