Canonical Allele Identifier: PA181611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178166
ClinVar RCV Id: RCV000154887 RCV000172616 RCV000852786 RCV001131361 RCV001131360 RCV001083749 RCV001131357 RCV001131358 RCV001131359 RCV002362817 RCV004544420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr31861Cys
CA181608
NM_001267550.2:c.95582A>G