Canonical Allele Identifier: PA140721
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47335
ClinVar RCV Id: RCV000040605 RCV000464020 RCV001093053 RCV001134503 RCV001171268 RCV001135950 RCV001134502 RCV001134504 RCV001135951 RCV001293087 RCV002336148 RCV004534928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg23371Trp
CA140718
NM_001256850.1:c.70111C>T