Canonical Allele Identifier: PA2826414575
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466970
ClinVar RCV Id: RCV000532413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile9013Val
CA1999681
NM_001256850.1:c.27037A>G