Canonical Allele Identifier: PA2830227111
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1439658
ClinVar RCV Id: RCV001958136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Lys26387Arg
CA349407302
NM_133432.3:c.79160A>G