Canonical Allele Identifier: PA2830204928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 509725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr66Met
CA2006395
NM_133378.4:c.197C>T