Canonical Allele Identifier: PA302732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 193962
ClinVar RCV Id: RCV000214411 RCV000724240 RCV000768887 RCV001085372 RCV004535198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val9359Ile
CA302729
NM_133378.4:c.28075G>A