Canonical Allele Identifier: PA2826425795
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29708Cys
CA178433
NM_001256850.1:c.89122C>T