Canonical Allele Identifier: PA645410513
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr20845Met
CA1992216
NM_001267550.2:c.62534C>T