Canonical Allele Identifier: PA203818
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 199241
ClinVar RCV Id: RCV000180762 RCV000232509 RCV000250709 RCV000769900 RCV001133626 RCV001135121 RCV001135123 RCV001133625 RCV001135122 RCV001721131 RCV004537519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg9516His
CA203815
NM_001267550.2:c.28547G>A