Canonical Allele Identifier: PA2826489385
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg1441His
CA2005336
NM_001267550.2:c.4322G>A