Canonical Allele Identifier: PA102187
Gene: WAS HGNC NCBI
ClinVar RCV:
RCV000011863
ClinVar Variation:
11114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000368.1:p.Arg86Leu
CA341001
NM_000377.3:c.257G>T