Canonical Allele Identifier: PA2830226377
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_597676.3:p.Leu25725Val
CA1985506
NM_133432.3:c.77173C>G
CA2825001004
NM_133432.3:c.77172_77173delinsGG