Canonical Allele Identifier: PA102223
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 135413
ClinVar RCV Id: RCV000122268 RCV000514559 RCV000990810 RCV001081710 RCV002280873 RCV003315781 RCV003975089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Glu131Lys
CA162684
NM_000377.3:c.391G>A