Canonical Allele Identifier: PA2741949976
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2993645
ClinVar RCV Id: RCV003853220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055908.1:p.Arg347Gln
CA4041475
NM_015093.6:c.1040G>A