Allele Registry

Canonical Allele Identifier: PA102342

Gene: WAS HGNC NCBI

ClinVar RCV:

RCV000011875

ClinVar Variation:

11126

HGVS (amino-acid)	Matching Registered Transcripts
NP_000368.1:p.Pro58Arg	CA121361 NM_000377.3:c.173C>G