Canonical Allele Identifier: PA138672
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46585
ClinVar RCV Id: RCV000039855 RCV000185316 RCV000554346 RCV000769089 RCV000619842 RCV001132041 RCV001132979 RCV001132980 RCV001132981 RCV001132982
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp3500Glu
CA138670
NM_133378.4:c.10500C>A
CA349602499
NM_133378.4:c.10500C>G