Canonical Allele Identifier: PA141141
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47479
ClinVar RCV Id: RCV000040748 RCV000723789 RCV001170314 RCV001084841 RCV001132651 RCV001132652 RCV001132653 RCV001132654 RCV001132655 RCV002354217 RCV004534935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val29487Met
CA141137
NM_001267550.2:c.88459G>A