Canonical Allele Identifier: PA181659
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96313
ClinVar RCV Id: RCV000154901 RCV000232949 RCV000619471 RCV000852798 RCV001128962 RCV001128958 RCV001128959 RCV001128960 RCV001128961 RCV001811390 RCV003486645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile27002Val
CA181657
NM_133378.4:c.81004A>G