Allele Registry

Canonical Allele Identifier: PA281106

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000022859

RCV001058962

RCV001268500

RCV003407355

ClinVar Variation:

29967

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Ile294Thr	CA281104 NM_000377.3:c.881T>C