Canonical Allele Identifier: PA181824
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178220
ClinVar RCV Id: RCV000154955 RCV000252544 RCV000467649 RCV001135957 RCV001134532 RCV001135955 RCV001135956 RCV001135958 RCV001697149 RCV001798508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys11090Arg
CA181823
NM_133378.4:c.33269A>G