Canonical Allele Identifier: PA140311
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_596869.4:p.Arg18738His
CA140309
NM_133378.4:c.56213G>A