Canonical Allele Identifier: PA236214
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 191190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Ser926Ile
CA236213
NM_025132.4:c.2777G>T