Canonical Allele Identifier: PA2825858796
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Ile583Lys
CA210283
NM_001143850.3:c.1748T>A