Canonical Allele Identifier: PA2830193579
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_596869.4:p.Ile8086Val
CA1999681
NM_133378.4:c.24256A>G