Canonical Allele Identifier: PA915962986
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 658817
ClinVar RCV Id: RCV000815707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro399Arg
CA412873480
NM_000377.3:c.1196C>G