Canonical Allele Identifier: PA139037
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46719
ClinVar RCV Id: RCV000039989 RCV000726274 RCV001130096 RCV001135129 RCV001135131 RCV001135128 RCV001135130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val7798Met
CA139034
NM_001267550.2:c.23392G>A