Canonical Allele Identifier: PA915962977
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 798158
ClinVar RCV Id: RCV001521520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Glu301Asp
CA10403999
NM_000377.3:c.903G>C
CA412872465
NM_000377.3:c.903G>T