Canonical Allele Identifier: PA309981
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_001243779.1:p.Val15284Ala
CA309980
NM_001256850.1:c.45851T>C