Canonical Allele Identifier: PA658659190
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466747
ClinVar RCV Id: RCV000552173 RCV002491028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35340Ser
CA1985179
NM_001267550.2:c.106018G>A