Canonical Allele Identifier: PA916066772
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_597681.4:p.Arg9164Trp
CA1993698
NM_133437.4:c.27490C>T