Canonical Allele Identifier: PA140886
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47398
ClinVar RCV Id: RCV000040668 RCV000620281 RCV000768913 RCV001086543 RCV000461664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile27180Thr
CA140882
NM_001267550.2:c.81539T>C