Allele Registry

Canonical Allele Identifier: PA162691

Gene: WAS HGNC NCBI

ClinVar Allele:

45573

ClinVar RCV:

RCV000030596

RCV000122270

RCV000419963

RCV001086760

RCV003914875

ClinVar Variation:

36912

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.His180Asn	CA162689 NM_000377.3:c.538C>A