Canonical Allele Identifier: PA658816117
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 519031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile27270Thr
CA1989152
NM_001267550.2:c.81809T>C