Canonical Allele Identifier: PA2826421147
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val21661Ile
CA140548
NM_001256850.1:c.64981G>A