Canonical Allele Identifier: PA310882
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202981
ClinVar RCV Id: RCV000714115 RCV000461669 RCV001170306 RCV002362958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg28826Cys
CA310881
NM_001256850.1:c.86476C>T