Canonical Allele Identifier: PA658816584
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala29851Asp
CA1987895
NM_001267550.2:c.89552C>A