Canonical Allele Identifier: PA658812774
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 504547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu5706Lys
CA2001913
NM_001267550.2:c.17116G>A