Canonical Allele Identifier: PA2826425918
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165717
ClinVar RCV Id: RCV000152182 RCV000477611 RCV000726542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29914His
CA178427
NM_001256850.1:c.89741G>A