Canonical Allele Identifier: PA141612
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47652
ClinVar RCV Id: RCV000040921 RCV000082470 RCV000622061 RCV000852775 RCV001130524 RCV001130525 RCV001130527 RCV001080039 RCV001130526 RCV001130528
ClinVar Variation Id: 796406
ClinVar RCV Id: RCV000979793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile32558Val
CA141609
NM_001256850.1:c.97672A>G
CA915942139
NM_001256850.1:c.97671_97672delinsTG