Canonical Allele Identifier: PA645410159
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413198
ClinVar RCV Id: RCV000595322 RCV001087627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe17754Ser
CA1993835
NM_001267550.2:c.53261T>C