Canonical Allele Identifier: PA2826819856
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1551556
ClinVar RCV Id: RCV002177967 RCV002553711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278963.1:p.His158Tyr
CA4041408
NM_001292034.3:c.472C>T