Canonical Allele Identifier: PA891846944
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 566906
ClinVar RCV Id: RCV000686843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Gln33Glu
CA412865716
NM_000377.3:c.97C>G