Canonical Allele Identifier: PA178374
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_001254479.2:p.Ser34010Arg
CA178372
NM_001267550.2:c.102028A>C
CA349418528
NM_001267550.2:c.102030T>G
CA349418529
NM_001267550.2:c.102030T>A