Canonical Allele Identifier: PA2580113898
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2159032
ClinVar RCV Id: RCV003085843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro356His
CA412873184
NM_000377.3:c.1067C>A