Canonical Allele Identifier: PA302570
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu1359Gly
CA302567
NM_001267550.2:c.4076A>G