Canonical Allele Identifier: PA2830241449
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47620
ClinVar RCV Id: RCV000040889 RCV000275108 RCV000269396 RCV000332789 RCV000326843 RCV000371058 RCV000464007 RCV000383950 RCV000768841 RCV001528790 RCV002381320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly24404Glu
CA141525
NM_133437.4:c.73211G>A