Canonical Allele Identifier: PA2830242019
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_597681.4:p.Ser25137Arg
CA178372
NM_133437.4:c.75409A>C
CA349418528
NM_133437.4:c.75411T>G
CA349418529
NM_133437.4:c.75411T>A