Canonical Allele Identifier: PA302444
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191887
ClinVar RCV Id: RCV000172246 RCV000545122 RCV002345594 RCV002500449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg26852His
CA302441
NM_001267550.2:c.80555G>A