Canonical Allele Identifier: PA309982
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202686
ClinVar RCV Id: RCV000220451 RCV000465576 RCV001133606 RCV001133607 RCV001133609 RCV001133608 RCV001133610 RCV001704903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val16925Ala
CA309980
NM_001267550.2:c.50774T>C