Canonical Allele Identifier: PA138646
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46573
ClinVar RCV Id: RCV000039843 RCV000464810 RCV000769835 RCV001509175 RCV002408527 RCV004534848
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys35918Tyr
CA138642
NM_001267550.2:c.107753G>A