Canonical Allele Identifier: PA211118
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165924
ClinVar RCV Id: RCV000152268 RCV000461956 RCV000618661 RCV001085555 RCV001132664 RCV001171295 RCV001132661 RCV001132662 RCV001132663 RCV001136052 RCV004532694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu17812Met
CA211117
NM_133378.4:c.53434C>A