Canonical Allele Identifier: PA2825858547
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2085374
ClinVar RCV Id: RCV003005031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Pro116Leu
CA6860876
NM_001143850.3:c.347C>T