Canonical Allele Identifier: PA2826419995
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467367
ClinVar RCV Id: RCV001130771 RCV001133736 RCV000549166 RCV001133738 RCV000593395 RCV002282219 RCV001130770 RCV001133737 RCV002456151
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val19662Met
CA1992002
NM_001256850.1:c.58984G>A