Canonical Allele Identifier: PA140075
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47126
ClinVar RCV Id: RCV000040396 RCV000118768 RCV000253459 RCV000467434 RCV000852835 RCV001135095 RCV001135096 RCV001135098 RCV001135097 RCV001135099 RCV001798164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu19196Val
CA140071
NM_001267550.2:c.57586C>G