Canonical Allele Identifier: PA2741816637
Gene: WAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2925929
ClinVar RCV Id: RCV003784023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Pro410Arg
CA412873546
NM_000377.3:c.1229C>G