Canonical Allele Identifier: PA2826413372
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala6598Ser
CA181898
NM_001256850.1:c.19792G>T