Canonical Allele Identifier: PA2741816634
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2944661
ClinVar RCV Id: RCV003808363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Gly379Arg
CA412873355
NM_000377.3:c.1135G>A
CA412873356
NM_000377.3:c.1135G>C