Canonical Allele Identifier: PA2826820100
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2175209
ClinVar RCV Id: RCV002579049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278964.1:p.Asn324Ser
CA4041480
NM_001292035.3:c.971A>G