Canonical Allele Identifier: PA2830210572
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly1157Ala
CA2005517
NM_133432.3:c.3470G>C