Canonical Allele Identifier: PA302623
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192159
ClinVar RCV Id: RCV000172645 RCV000222300 RCV000242642 RCV000475296 RCV000768939 RCV001132543 RCV001132544 RCV001129848 RCV001132542 RCV001132541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg21111Lys
CA302622
NM_133378.4:c.63332G>A