Canonical Allele Identifier: PA178373
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165653
ClinVar RCV Id: RCV000152161
ClinVar Variation Id: 535456
ClinVar RCV Id: RCV000643441 RCV002483847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser31442Arg
CA178372
NM_133378.4:c.94324A>C
CA349418528
NM_133378.4:c.94326T>G
CA349418529
NM_133378.4:c.94326T>A