Canonical Allele Identifier: PA2573169089
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1404643
ClinVar RCV Id: RCV001899058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Asp264Asn
CA412872175
NM_000377.3:c.790G>A