Canonical Allele Identifier: PA645411860
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg29505His
CA1988138
NM_001267550.2:c.88514G>A