Allele Registry

Canonical Allele Identifier: PA102236

Gene: WAS HGNC NCBI

ClinVar Allele:

535002

ClinVar RCV:

RCV000633307

RCV000657918

RCV003991033

ClinVar Variation:

528222

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Glu31Lys	CA412865672 NM_000377.3:c.91G>A