Canonical Allele Identifier: PA2829439601
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165813
ClinVar RCV Id: RCV000152207 RCV000273789 RCV000270152 RCV000325455 RCV000364915 RCV000369763 RCV000617421 RCV000471832 RCV000769931 RCV000852807 RCV001530137 RCV004532690
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile17836Val
CA248764
NM_003319.4:c.53506A>G