Canonical Allele Identifier: PA2826820097
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2993645
ClinVar RCV Id: RCV003853220
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278964.1:p.Arg315Gln
CA4041475
NM_001292035.3:c.944G>A