Canonical Allele Identifier: PA178741
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg15455Gln
CA178740
NM_133378.4:c.46364G>A