Canonical Allele Identifier: PA645409837
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg14996His
CA1995521
NM_001267550.2:c.44987G>A