Canonical Allele Identifier: PA309831
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg14967Gln
CA309829
NM_001267550.2:c.44900G>A