Canonical Allele Identifier: PA2826489376
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg1403Thr
CA2005386
NM_001267550.2:c.4208G>C