Canonical Allele Identifier: PA141436
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47585
ClinVar RCV Id: RCV000726674 RCV001088882 RCV000040854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg29905His
CA141434
NM_133378.4:c.89714G>A