Canonical Allele Identifier: PA272719
Gene: TCTN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 160100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001076007.1:p.Ala314Thr
CA272717
NM_001082538.3:c.940G>A