Canonical Allele Identifier: PA151407
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 127155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Asp493His
CA151406
NM_025132.4:c.1477G>C