Canonical Allele Identifier: PA658810229
Gene: TCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 440324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171655.1:p.Gly94Ser
CA10184571
NM_001184726.2:c.280G>A