Canonical Allele Identifier: PA2830211198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 496991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala1868Thr
CA2005144
NM_133432.3:c.5602G>A