Canonical Allele Identifier: PA2826429089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1397267
ClinVar RCV Id: RCV001906061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile33819Val
CA349405629
NM_001256850.1:c.101455A>G