Canonical Allele Identifier: PA140444
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47245
ClinVar RCV Id: RCV000040515 RCV000464443 RCV001703905 RCV001839672 RCV001839674 RCV001839673 RCV001839675 RCV002371844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys20685Arg
CA140441
NM_001256850.1:c.62054A>G