Canonical Allele Identifier: PA658666776
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg23636Cys
CA1990707
NM_001267550.2:c.70906C>T