Canonical Allele Identifier: PA311784
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203241
ClinVar RCV Id: RCV000591089 RCV000726948 RCV001087944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro4930Thr
CA311782
NM_001267550.2:c.14788C>A