Canonical Allele Identifier: PA2829445093
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_003310.4:p.Leu25600Val
CA1985506
NM_003319.4:c.76798C>G
CA2825001004
NM_003319.4:c.76797_76798delinsGG