Canonical Allele Identifier: PA916066758
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332834
ClinVar RCV Id: RCV000261639 RCV000297342 RCV000356804 RCV000350885 RCV000395016 RCV000868806 RCV001551202 RCV002450900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala9140Ser
CA1993706
NM_133437.4:c.27418G>T