Canonical Allele Identifier: PA141587
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47645
ClinVar RCV Id: RCV000040914 RCV000713952 RCV000769853 RCV000852777 RCV001084745 RCV001128724 RCV001128725 RCV001128726 RCV001128723 RCV001135717 RCV002390171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp32394Asn
CA141584
NM_001256850.1:c.97180G>A