Canonical Allele Identifier: PA2741816621
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2949280
ClinVar RCV Id: RCV003802006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Arg273Ser
CA412872234
NM_000377.3:c.819G>C
CA412872235
NM_000377.3:c.819G>T