Canonical Allele Identifier: PA141167
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47489
ClinVar RCV Id: RCV000040758 RCV000172208 RCV001082145 RCV001134228 RCV001134225 RCV001134226 RCV001134227 RCV001134229 RCV001798193 RCV002362637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg29809Gln
CA141163
NM_001267550.2:c.89426G>A