Canonical Allele Identifier: PA2580113886
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1705081
ClinVar RCV Id: RCV002283406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Leu267Arg
CA412872201
NM_000377.3:c.800T>G