Canonical Allele Identifier: PA140238
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47177
ClinVar RCV Id: RCV000040447 RCV000172651 RCV000300024 RCV000279995 RCV000335020 RCV000378989 RCV000401779 RCV000621320 RCV000768965 RCV000852829 RCV001084857 RCV002222152 RCV004534916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg19000Gln
CA140235
NM_001256850.1:c.56999G>A