Canonical Allele Identifier: PA2826705025
Gene: TBCE HGNC NCBI

Linked Data

ClinVar Variation Id: 193652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274731.1:p.Ile170Phe
CA239231
NM_001287802.2:c.508A>T