Canonical Allele Identifier: PA2826489467
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497010
ClinVar RCV Id: RCV000592201 RCV001128781 RCV001131430 RCV001131431 RCV001131432 RCV001128780 RCV001170106 RCV002367996
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg2120Gln
CA2005064
NM_001267550.2:c.6359G>A