Canonical Allele Identifier: PA2830203860
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332694
ClinVar Variation Id: 3223359
ClinVar RCV Id: RCV004508714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu32097Val
CA1985506
NM_133378.4:c.96289C>G
CA2825001004
NM_133378.4:c.96288_96289delinsGG