Canonical Allele Identifier: PA346748
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180565
ClinVar RCV Id: RCV000157552 RCV000726498
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val3319Ile
CA346745
NM_133378.4:c.9955G>A