ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826820041
Gene: TAB2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV002177967
RCV002553711
ClinVar Variation:
1551556
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001278964.1:p.His126Tyr
CA4041408
NM_001292035.3:c.376C>T