Canonical Allele Identifier: PA2826492729
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile10486Phe
CA1998946
NM_001267550.2:c.31456A>T