Canonical Allele Identifier: PA2580113890
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1956514
ClinVar RCV Id: RCV002720272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Glu306Lys
CA412872519
NM_000377.3:c.916G>A