Canonical Allele Identifier: PA141728
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47690
ClinVar RCV Id: RCV000040959 RCV000172151 RCV001132330 RCV001132332 RCV001132331 RCV001132333 RCV001133260 RCV002483020 RCV002408537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32571Ile
CA141726
NM_133378.4:c.97712C>T