Canonical Allele Identifier: PA302892
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196068
ClinVar RCV Id: RCV000220460 RCV000302870 RCV000356701 RCV000357762 RCV000402442 RCV000468138 RCV000406858 RCV000769924 RCV002345608 RCV001796725 RCV004537413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn26131Ile
CA302890
NM_001256850.1:c.78392A>T