Canonical Allele Identifier: PA140362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47213
ClinVar RCV Id: RCV000040483 RCV000082419 RCV000852822 RCV000620024 RCV001134836 RCV001134837 RCV001134839 RCV001079485 RCV001134838 RCV001134840 RCV001798173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val21597Met
CA140358
NM_001267550.2:c.64789G>A