Canonical Allele Identifier: PA2826429056
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1044177
ClinVar RCV Id: RCV001348389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile33781Thr
CA349406381
NM_001256850.1:c.101342T>C