Canonical Allele Identifier: PA2830208602
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val10709Ile
CA1996724
NM_133378.4:c.32125G>A