Canonical Allele Identifier: PA310711
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg26681Cys
CA310710
NM_001256850.1:c.80041C>T