Canonical Allele Identifier: PA141783
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47722
ClinVar RCV Id: RCV000040991 RCV000621101 RCV000466809 RCV001135817 RCV001135818 RCV001135819 RCV001135820 RCV001703920 RCV001134356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35869Gly
CA141780
NM_001267550.2:c.107605A>G