Canonical Allele Identifier: PA2830196968
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile17046Thr
CA1992767
NM_133378.4:c.51137T>C