Canonical Allele Identifier: PA2741816623
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2925671
ClinVar RCV Id: RCV003783765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Met307Val
CA412872531
NM_000377.3:c.919A>G