Canonical Allele Identifier: PA139667
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46969
ClinVar RCV Id: RCV000040239 RCV000473565 RCV000724718 RCV001133884 RCV001135397 RCV001135396 RCV002399388 RCV001135394 RCV001135395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg11958Gln
CA139665
NM_133378.4:c.35873G>A