Canonical Allele Identifier: PA139524
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46918
ClinVar RCV Id: RCV000040188 RCV000465574 RCV001170386 RCV001839598 RCV002504909 RCV003137564 RCV001839596 RCV001839597 RCV001839599 RCV004541150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro13029Thr
CA139521
NM_001267550.2:c.39085C>A