Canonical Allele Identifier: PA183638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179055
ClinVar RCV Id: RCV000155839 RCV000643751 RCV001134861 RCV001134863 RCV001134865 RCV001134862 RCV001134864 RCV004546442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile8025Met
CA183635
NM_001267550.2:c.24075T>G