Allele Registry

Canonical Allele Identifier: PA102178

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000011864

RCV000414284

RCV000633305

ClinVar Variation:

11115

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Arg86His	CA341003 NM_000377.3:c.257G>A