Canonical Allele Identifier: PA2830215031
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229449
ClinVar RCV Id: RCV000216081 RCV000253790 RCV000725245 RCV000852848 RCV001085087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro7980Ala
CA1994319
NM_133432.3:c.23938C>G