Canonical Allele Identifier: PA2830237781
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47423
ClinVar RCV Id: RCV000040693 RCV000725532 RCV001087252 RCV002345322 RCV003149659 RCV004534934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro18894Thr
CA140951
NM_133437.4:c.56680C>A