Allele Registry

Canonical Allele Identifier: PA102281

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000011876

ClinVar Variation:

11127

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Ile481Asn	CA121363 NM_000377.3:c.1442T>A