Canonical Allele Identifier: PA2830209989
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly586Asp
CA2005945
NM_133432.3:c.1757G>A