Canonical Allele Identifier: PA2580113896
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2047692
ClinVar RCV Id: RCV002926919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Gly334Asp
CA10404029
NM_000377.3:c.1001G>A