Canonical Allele Identifier: PA2826704411
Gene: TBCE HGNC NCBI

Linked Data

ClinVar Variation Id: 286377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274730.1:p.Pro72Ser
CA1463972
NM_001287801.2:c.214C>T