Canonical Allele Identifier: PA140687
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47322
ClinVar RCV Id: RCV000040592 RCV000247787 RCV000301041 RCV000314072 RCV000336155 RCV000458685 RCV000367543 RCV000396511 RCV000769945 RCV001083733 RCV002223143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu24609Gln
CA140683
NM_001267550.2:c.73825G>C