Canonical Allele Identifier: PA2573169132
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1404684
ClinVar RCV Id: RCV001901764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Leu434Phe
CA10404070
NM_000377.3:c.1300C>T