Canonical Allele Identifier: PA2830220135
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202874
ClinVar RCV Id: RCV000223093 RCV000338766 RCV000342317 RCV000312841 RCV000395107 RCV000297719 RCV000398493 RCV000714096 RCV000852810 RCV001079555 RCV004539724 RCV002336490 RCV003150073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg16701His
CA310554
NM_133432.3:c.50102G>A