Canonical Allele Identifier: PA2829442178
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179038
ClinVar RCV Id: RCV000155822 RCV000172198 RCV000286331 RCV000282938 RCV000380708 RCV000322760 RCV000377371 RCV000466689 RCV002362824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val21871Ile
CA183583
NM_003319.4:c.65611G>A