Canonical Allele Identifier: PA302861
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_001243779.1:p.Gly17814Ser
CA302859
NM_001256850.1:c.53440G>A