Canonical Allele Identifier: PA2573287347
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Val817Glu
CA2892085
NM_025132.4:c.2450T>A