Canonical Allele Identifier: PA102361
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 11122
ClinVar RCV Id: RCV000011871 RCV001509116
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Ser82Pro
CA121359
NM_000377.3:c.244T>C