Canonical Allele Identifier: PA645411649
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys28514Met
CA10613227
NM_001267550.2:c.85541A>T