Canonical Allele Identifier: PA139362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46853
ClinVar RCV Id: RCV000040123 RCV000725032 RCV001131660 RCV001131661 RCV001131663 RCV001170626 RCV001085078 RCV001131662 RCV001131664 RCV004534887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro10269Gln
CA139360
NM_001256850.1:c.30806C>A