Allele Registry

Canonical Allele Identifier: PA2573265826

Gene: TAB2 HGNC NCBI

ClinVar RCV:

RCV002177967

RCV002553711

ClinVar Variation:

1551556

HGVS (amino-acid)	Matching Registered Transcripts
NP_055908.1:p.His158Tyr	CA4041408 NM_015093.6:c.472C>T