Canonical Allele Identifier: PA2826423489
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516347
ClinVar RCV Id: RCV000605403 RCV000643071 RCV001135733 RCV001702686 RCV001128736 RCV001128737 RCV001135732 RCV001135734 RCV002343157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp25855Asn
CA1989062
NM_001256850.1:c.77563G>A