Canonical Allele Identifier: PA2826705057
Gene: TBCE HGNC NCBI

Linked Data

ClinVar Variation Id: 235262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274731.1:p.Ser220Thr
CA1464313
NM_001287802.2:c.659G>C