Canonical Allele Identifier: PA2825858510
Gene: TCTN2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Ala57Val
CA387155132
NM_001143850.3:c.170C>T