Canonical Allele Identifier: PA2825858498
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1435137
ClinVar RCV Id: RCV001972117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Pro31Leu
CA387154981
NM_001143850.3:c.92C>T