Canonical Allele Identifier: PA102151
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 11116
ClinVar RCV Id: RCV002243636 RCV001563489 RCV003764557 RCV000011865
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Ala56Val
CA255723
NM_000377.3:c.167C>T