Canonical Allele Identifier: PA1139669001
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 972434
ClinVar RCV Id: RCV001248465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Leu425_Ala426delinsProGly
CA1139667533
NM_000377.3:c.1272_1277delinsGCCTGG