Canonical Allele Identifier: PA281106
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 29967
ClinVar RCV Id: RCV000022859 RCV001058962 RCV001268500 RCV003407355
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Ile294Thr
CA281104
NM_000377.3:c.881T>C