Canonical Allele Identifier: PA2825160222
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 3189514
ClinVar RCV Id: RCV004477872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Asp296Asn
CA412872391
NM_000377.3:c.886G>A