Canonical Allele Identifier: PA2580466218
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2483870
ClinVar RCV Id: RCV003212055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Ala1180Thr
CA356647430
NM_025132.4:c.3538G>A