Canonical Allele Identifier: PA140313
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47201
ClinVar RCV Id: RCV000040471 RCV000172287 RCV001086239 RCV001130768 RCV001130767 RCV001130769 RCV001170812 RCV002453331 RCV001130765 RCV001130766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21306His
CA140309
NM_001267550.2:c.63917G>A