Canonical Allele Identifier: PA181911
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178248
ClinVar RCV Id: RCV000154987 RCV000232825 RCV000724663 RCV001132363 RCV001129647 RCV001129645 RCV001129646 RCV001132364
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr6339Cys
CA181908
NM_001267550.2:c.19016A>G