Canonical Allele Identifier: PA302381
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33523Cys
CA302379
NM_001256850.1:c.100567C>T