Canonical Allele Identifier: PA178443
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165735
ClinVar RCV Id: RCV000152188 RCV000172199 RCV000309213 RCV000269133 RCV000367439 RCV000326590 RCV000402112 RCV000619946 RCV000642884 RCV001798477
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg30895Gln
CA178440
NM_001267550.2:c.92684G>A