Canonical Allele Identifier: PA283713
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47297
ClinVar RCV Id: RCV000040567 RCV000204975 RCV000265924 RCV000250798 RCV000285494 RCV000321007 RCV000345056 RCV000381017 RCV000770129 RCV001353375 RCV002227054 RCV004541173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ile2118Thr
CA283707
NM_133379.5:c.6353T>C