Canonical Allele Identifier: PA181877
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178236
ClinVar RCV Id: RCV000154973 RCV000287568 RCV000326198 RCV000327268 RCV000384268 RCV000387819 RCV000725482 RCV001084561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg6745Cys
CA181876
NM_133378.4:c.20233C>T