Canonical Allele Identifier: PA181893
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178242
ClinVar RCV Id: RCV000154980 RCV000172692 RCV000473052 RCV000852895 RCV001170082 RCV004534978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys6866Tyr
CA181891
NM_001256850.1:c.20597G>A