Canonical Allele Identifier: PA140655
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg21595His
CA140653
NM_133378.4:c.64784G>A