Canonical Allele Identifier: PA2826820102
Gene: TAB2 HGNC NCBI
ClinVar RCV:
RCV001893857
ClinVar Variation:
1399671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278964.1:p.Ser325Thr
CA4041483
NM_001292035.3:c.974G>C