Canonical Allele Identifier: PA915962983
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 798143
ClinVar RCV Id: RCV001484626 RCV003307780
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Ala350Val
CA412873120
NM_000377.3:c.1049C>T