Canonical Allele Identifier: PA2573169092
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1432520
ClinVar RCV Id: RCV001982034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Ser269Cys
CA412872207
NM_000377.3:c.805A>T