Canonical Allele Identifier: PA2825858687
Gene: TCTN2 HGNC NCBI
ClinVar RCV:
RCV003813391
ClinVar Variation:
2954168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Ile362Thr
CA387141110
NM_001143850.3:c.1085T>C