Canonical Allele Identifier: PA645410190
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229462
ClinVar RCV Id: RCV000218519 RCV000473378 RCV000834830 RCV001132768 RCV001132765 RCV001132767 RCV001132764 RCV001132766 RCV002450637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg18037Trp
CA1993698
NM_001267550.2:c.54109C>T