Canonical Allele Identifier: PA1139669006
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 950368
ClinVar RCV Id: RCV001222061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Arg439Pro
CA412873709
NM_000377.3:c.1316G>C