Canonical Allele Identifier: PA310619
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202895
ClinVar RCV Id: RCV000184862 RCV000323369 RCV000270696 RCV000283370 RCV000380163 RCV000322095 RCV001085916 RCV002345656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg26619His
CA310617
NM_001267550.2:c.79856G>A