Canonical Allele Identifier: PA2825858592
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 126288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Arg199Gln
CA150964
NM_001143850.3:c.596G>A