Canonical Allele Identifier: PA645410113
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu17400Ala
CA1994035
NM_001267550.2:c.52199A>C