Canonical Allele Identifier: PA302386
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg35043His
CA302383
NM_001267550.2:c.105128G>A