Canonical Allele Identifier: PA358821
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132133
ClinVar RCV Id: RCV000119021 RCV000254991 RCV000627779 RCV000768851 RCV002250566 RCV003989320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys31712Arg
CA358820
NM_001267550.2:c.95134T>C