Canonical Allele Identifier: PA2830190364
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met113Val
CA16610652
NM_133378.4:c.337A>G