Canonical Allele Identifier: PA140398
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47229
ClinVar RCV Id: RCV000040499 RCV000241625 RCV000282835 RCV000337921 RCV000381175 RCV000341241 RCV000408381 RCV000466378 RCV001170583 RCV001703903 RCV004528213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21916Gln
CA140394
NM_001267550.2:c.65747G>A