Canonical Allele Identifier: PA140656
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg22522His
CA140653
NM_001256850.1:c.67565G>A