Canonical Allele Identifier: PA2580113884
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2058862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Gln255His
CA10403980
NM_000377.3:c.765G>C
CA412872106
NM_000377.3:c.765G>T