Canonical Allele Identifier: PA658667156
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser26305Cys
CA1989553
NM_001267550.2:c.78914C>G