Canonical Allele Identifier: PA2830227241
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_597676.3:p.Ile26520Val
CA349405629
NM_133432.3:c.79558A>G