Canonical Allele Identifier: PA341212
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu35956Pro
CA341209
NM_001267550.2:c.107867T>C