Canonical Allele Identifier: PA2825858506
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3175381
ClinVar RCV Id: RCV004466710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Thr49Ser
CA15743462
NM_001143850.3:c.146C>G
CA387155086
NM_001143850.3:c.145A>T