Canonical Allele Identifier: PA2830227122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191810
ClinVar RCV Id: RCV000172149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu26403Gly
CA237605
NM_133432.3:c.79208A>G