Canonical Allele Identifier: PA645410016
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu16469His
CA1994604
NM_001267550.2:c.49406T>A