Canonical Allele Identifier: PA2826819917
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399671
ClinVar RCV Id: RCV001893857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278963.1:p.Ser357Thr
CA4041483
NM_001292034.3:c.1070G>C