Canonical Allele Identifier: PA140458
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly22383Arg
CA140455
NM_001267550.2:c.67147G>A
CA349424385
NM_001267550.2:c.67147G>C