Canonical Allele Identifier: PA2825858601
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 307550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Asn211Ser
CA6860949
NM_001143850.3:c.632A>G