Canonical Allele Identifier: PA2573265869
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399671
ClinVar RCV Id: RCV001893857
JSON-LD

Amino-acid Alleles

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