Canonical Allele Identifier: PA289119
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130688
ClinVar RCV Id: RCV000118797 RCV000317280 RCV000313328 RCV000355456 RCV001293103 RCV000273543 RCV000319315 RCV001082250 RCV000395255 RCV002444573 RCV001798370 RCV004542865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg3113His
CA289115
NM_001267550.2:c.9338G>A