Canonical Allele Identifier: PA1139668995
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 844565
ClinVar RCV Id: RCV001047443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro392Thr
CA329102334
NM_000377.3:c.1174C>A