Canonical Allele Identifier: PA2830227722
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Leu27016Pro
CA341209
NM_133432.3:c.81047T>C