Canonical Allele Identifier: PA645409658
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13143Ile
CA1996724
NM_001267550.2:c.39427G>A