Canonical Allele Identifier: PA2826411954
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466795
ClinVar RCV Id: RCV000559272 RCV001570411 RCV002456140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu3687Gly
CA2002775
NM_001256850.1:c.11060A>G