Canonical Allele Identifier: PA2830216648
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130675
ClinVar RCV Id: RCV000118771 RCV000556436 RCV001132252 RCV001132253 RCV001132254 RCV001133162 RCV001133163 RCV002321598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly10810Ser
CA231599
NM_133432.3:c.32428G>A