Allele Registry

Canonical Allele Identifier: PA102223

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000122268

RCV000514559

RCV000990810

RCV001081710

RCV002280873

RCV003315781

RCV003975089

ClinVar Variation:

135413

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Glu131Lys	CA162684 NM_000377.3:c.391G>A