Canonical Allele Identifier: PA2825858582
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 307548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Ser190Ala
CA6860932
NM_001143850.3:c.568T>G