Canonical Allele Identifier: PA645409662
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu13157Lys
CA1996692
NM_001267550.2:c.39469G>A