Canonical Allele Identifier: PA645410121
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332841
ClinVar RCV Id: RCV000260068 RCV000314067 RCV000317569 RCV000371115 RCV000396717 RCV002298571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile17478Met
CA1993989
NM_001267550.2:c.52434T>G