Canonical Allele Identifier: PA2741986719
Gene: TCTN2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079085.2:p.Ile363Thr
CA387141110
NM_024809.5:c.1088T>C