Canonical Allele Identifier: PA2573265869
Gene: TAB2 HGNC NCBI
ClinVar RCV:
RCV001893857
ClinVar Variation:
1399671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055908.1:p.Ser357Thr
CA4041483
NM_015093.6:c.1070G>C