Canonical Allele Identifier: PA2830227119
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2921699
ClinVar RCV Id: RCV003782721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly26400Val
CA349407206
NM_133432.3:c.79199G>T