Canonical Allele Identifier: PA302873
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196004
ClinVar RCV Id: RCV000724201 RCV000705326 RCV002372089 RCV004537411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe20576Cys
CA302871
NM_001256850.1:c.61727T>G