Allele Registry

Canonical Allele Identifier: PA645506032

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000482823

RCV000780796

RCV001038563

ClinVar Variation:

418541

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Asp485Asn	CA16621420 NM_000377.3:c.1453G>A