Canonical Allele Identifier: PA141153
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47483
ClinVar RCV Id: RCV000040752 RCV000282040 RCV000348715 RCV000352269 RCV000374104 RCV000386956 RCV000725034 RCV001170313 RCV001085079 RCV002354219 RCV004534937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg27933His
CA141150
NM_001256850.1:c.83798G>A