Allele Registry

Canonical Allele Identifier: PA645505846

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000485571

ClinVar Variation:

420291

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Pro58His	CA16621416 NM_000377.3:c.173C>A