Canonical Allele Identifier: PA916016958
Gene: TBCE HGNC NCBI

Linked Data

ClinVar Variation Id: 193652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274730.1:p.Ile334Phe
CA239231
NM_001287801.2:c.1000A>T