Canonical Allele Identifier: PA2830208797
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val11262Ile
CA309778
NM_133378.4:c.33784G>A