Canonical Allele Identifier: PA310147
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202742
ClinVar RCV Id: RCV000184664 RCV000460043 RCV000619810 RCV001132250 RCV001132251 RCV001132248 RCV001132247 RCV001132249 RCV001532422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn18120Ser
CA310146
NM_001256850.1:c.54359A>G