Canonical Allele Identifier: PA2830198732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp21149Tyr
CA1990672
NM_133378.4:c.63445G>T