Canonical Allele Identifier: PA203816
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 199241
ClinVar RCV Id: RCV000180762 RCV000232509 RCV000250709 RCV000769900 RCV001133626 RCV001135121 RCV001135123 RCV001133625 RCV001135122 RCV001721131 RCV004537519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg8272His
CA203815
NM_133378.4:c.24815G>A