Canonical Allele Identifier: PA140863
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47387
ClinVar RCV Id: RCV000040657 RCV000466151 RCV000836494 RCV002345314
ClinVar Variation Id: 167766
ClinVar RCV Id: RCV000259093 RCV001132949 RCV000723773 RCV001132948 RCV001132950 RCV001132946 RCV001132947 RCV003764943 RCV002345491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg24284Cys
CA140861
NM_133378.4:c.72849_72850delinsTT
CA295646
NM_133378.4:c.72850C>T