Allele Registry

Canonical Allele Identifier: PA102361

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000011871

RCV001509116

ClinVar Variation:

11122

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Ser82Pro	CA121359 NM_000377.3:c.244T>C