Canonical Allele Identifier: PA302862
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 195843
ClinVar RCV Id: RCV000176513 RCV000218113 RCV000245462 RCV000537285 RCV001132558 RCV001133469 RCV001132557 RCV001132559 RCV001132560 RCV003486729 RCV004537403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly19455Ser
CA302859
NM_001267550.2:c.58363G>A