Allele Registry

Canonical Allele Identifier: PA102292

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000011874

RCV001291553

RCV001851800

ClinVar Variation:

11125

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Leu270Pro	CA280988 NM_000377.3:c.809T>C