Canonical Allele Identifier: PA2573169106
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1450023
ClinVar RCV Id: RCV001989933 RCV002563576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Ile331Phe
CA412872872
NM_000377.3:c.991A>T