Canonical Allele Identifier: PA2826493136
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu2173Val
CA2005016
NM_001267550.2:c.6517T>G