Canonical Allele Identifier: PA2826429102
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1463137
ClinVar RCV Id: RCV001960902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33832Glu
CA349405393
NM_001256850.1:c.101495G>A