Canonical Allele Identifier: PA645410220
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val18240Ile
CA1993584
NM_001267550.2:c.54718G>A