Canonical Allele Identifier: PA289113
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130687
ClinVar RCV Id: RCV000118796 RCV000279980 RCV000284327 RCV000337342 RCV000407424 RCV000407478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Trp31798Arg
CA289110
NM_001256850.1:c.95392T>C
CA349426288
NM_001256850.1:c.95392T>A