Canonical Allele Identifier: PA2499231853
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1010931
ClinVar RCV Id: RCV001308651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro359Ser
CA412873215
NM_000377.3:c.1075C>T