Canonical Allele Identifier: PA2580113909
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1951247
ClinVar RCV Id: RCV002694980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Leu425Pro
CA412873627
NM_000377.3:c.1274T>C