Canonical Allele Identifier: PA2830192730
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met5867Thr
CA311951
NM_133378.4:c.17600T>C