Canonical Allele Identifier: PA310097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202725
ClinVar RCV Id: RCV000222884 RCV000727052 RCV001086041 RCV002433829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg18473Gly
CA310095
NM_001267550.2:c.55417A>G