Canonical Allele Identifier: PA2826414617
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1315137
ClinVar RCV Id: RCV001773331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser9064Cys
CA1999653
NM_001256850.1:c.27191C>G