Canonical Allele Identifier: PA658665218
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466964
ClinVar RCV Id: RCV000547639 RCV002285358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser9223Pro
CA1999746
NM_001267550.2:c.27667T>C