Canonical Allele Identifier: PA183459
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178998
ClinVar RCV Id: RCV000155776 RCV000244691 RCV000934827 RCV001170574 RCV001288921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr20353Ile
CA183458
NM_133378.4:c.61058C>T