Canonical Allele Identifier: PA2830191362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg2320His
CA236104
NM_133378.4:c.6959G>A