Canonical Allele Identifier: PA2830227250
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2072287
ClinVar RCV Id: RCV002949529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Leu26528Val
CA349405502
NM_133432.3:c.79582C>G