Canonical Allele Identifier: PA891846962
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 567298
ClinVar RCV Id: RCV000687335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Leu419Met
CA412873591
NM_000377.3:c.1255C>A