Canonical Allele Identifier: PA2828334042
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2175209
ClinVar RCV Id: RCV002579049
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356435.1:p.Asn356Ser
CA4041480
NM_001369506.1:c.1067A>G