Allele Registry

Canonical Allele Identifier: PA2580465746

Gene: WDR19 HGNC NCBI

ClinVar Variation Id: 2007938

HGVS (amino-acid)	Matching Registered Transcripts
NP_079408.3:p.Ser280Arg	CA356634478 NM_025132.4:c.838A>C CA356634484 NM_025132.4:c.840C>A CA356634485 NM_025132.4:c.840C>G