Canonical Allele Identifier: PA139761
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47010
ClinVar RCV Id: RCV000040280 RCV000225870 RCV000254435 RCV000343876 RCV000352447 RCV000308756 RCV000404240 RCV000392384 RCV000852855 RCV001083111 RCV001798152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg15772Gln
CA139757
NM_001267550.2:c.47315G>A