Canonical Allele Identifier: PA1139668996
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 962220
ClinVar RCV Id: RCV001236034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro400Leu
CA10404048
NM_000377.3:c.1199C>T