Canonical Allele Identifier: PA2826489282
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg648Thr
CA2005931
NM_001267550.2:c.1943G>C