Canonical Allele Identifier: PA2830217229
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202761
ClinVar RCV Id: RCV000184691 RCV000229909 RCV001135743 RCV001134248 RCV001134249 RCV001134250 RCV001135742 RCV001171288 RCV002453679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala11869Thr
CA310203
NM_133432.3:c.35605G>A