Canonical Allele Identifier: PA2830227115
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1505993
ClinVar RCV Id: RCV002035882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Tyr26396Asp
CA60953516
NM_133432.3:c.79186T>G