Canonical Allele Identifier: PA309038
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202307
ClinVar RCV Id: RCV000184146 RCV000467045 RCV001704890 RCV002444747 RCV003486744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg14229His
CA309037
NM_133378.4:c.42686G>A