Canonical Allele Identifier: PA311126
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg33738His
CA311124
NM_001267550.2:c.101213G>A