Canonical Allele Identifier: PA645410397
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 289524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu19781Phe
CA1992686
NM_001267550.2:c.59341C>T