Canonical Allele Identifier: PA658666123
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr19692Ala
CA1992720
NM_001267550.2:c.59074A>G