Canonical Allele Identifier: PA2826414477
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr8845Met
CA1999797
NM_001256850.1:c.26534C>T