Canonical Allele Identifier: PA139914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47070
ClinVar RCV Id: RCV000040340 RCV000172663 RCV000291245 RCV000350259 RCV000315170 RCV000335069 RCV000404069 RCV000770012 RCV000618788 RCV000852844 RCV001086451 RCV002221192 RCV004534906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg15131His
CA139912
NM_133378.4:c.45392G>A