Canonical Allele Identifier: PA141676
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47672
ClinVar RCV Id: RCV000040941 RCV002399393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32237Leu
CA141674
NM_133378.4:c.96710G>T