Canonical Allele Identifier: PA2580113908
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2319059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro416Leu
CA412873580
NM_000377.3:c.1247C>T