Canonical Allele Identifier: PA102371
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 11123
ClinVar RCV Id: RCV000011872 RCV000851684 RCV001037597 RCV001172206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Thr45Met
CA255728
NM_000377.3:c.134C>T