Canonical Allele Identifier: PA309066
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu20773Met
CA309064
NM_001267550.2:c.62317C>A