Allele Registry

Canonical Allele Identifier: PA255727

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000011866

ClinVar Variation:

11117

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Ala236Gly	CA255725 NM_000377.3:c.707C>G