Canonical Allele Identifier: PA311152
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203071
ClinVar RCV Id: RCV000185092 RCV000462205 RCV000727152 RCV001131014 RCV001131015 RCV001130308 RCV001130307 RCV001130309 RCV002390483
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile32836Thr
CA311151
NM_001256850.1:c.98507T>C