Canonical Allele Identifier: PA162688
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 135414
ClinVar RCV Id: RCV000122269 RCV000862741 RCV001261849 RCV003436938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Arg138Gln
CA162686
NM_000377.3:c.413G>A