Canonical Allele Identifier: PA2499231846
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1013735
ClinVar RCV Id: RCV001312371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Thr282Ala
CA412872292
NM_000377.3:c.844A>G