Canonical Allele Identifier: PA139089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46741
ClinVar RCV Id: RCV000040011 RCV000082378 RCV001085022 RCV001170867 RCV001132271 RCV001132267 RCV001132268 RCV001132269 RCV001132270 RCV001787037 RCV004534874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu7030Lys
CA139087
NM_133378.4:c.21088G>A