Canonical Allele Identifier: PA302958
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196801
ClinVar RCV Id: RCV000177667 RCV000221018 RCV000620787 RCV000770121 RCV001080643 RCV001131079 RCV001134033 RCV001131080 RCV001131081 RCV001131082 RCV003227694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His2508Arg
CA302955
NM_001267550.2:c.7523A>G