Canonical Allele Identifier: PA2826425926
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1329220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val29930Met
CA60972536
NM_001256850.1:c.89788G>A