Canonical Allele Identifier: PA2830219187
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404701
ClinVar RCV Id: RCV000465920 RCV000842647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile15020Thr
CA1990576
NM_133432.3:c.45059T>C