Canonical Allele Identifier: PA2830191192
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 496991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala1914Thr
CA2005144
NM_133378.4:c.5740G>A