Canonical Allele Identifier: PA140289
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47195
ClinVar RCV Id: RCV000040465 RCV000459694 RCV000725302 RCV001798170 RCV002345306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg1861His
CA140284
NM_133378.4:c.5582G>A