Canonical Allele Identifier: PA2830054159
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2011941
ClinVar RCV Id: RCV002838786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Arg244Pro
CA356634247
NM_025132.4:c.731G>C