Canonical Allele Identifier: PA2499231845
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1018255
ClinVar RCV Id: RCV001317528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Arg268Trp
CA10403991
NM_000377.3:c.802C>T