Canonical Allele Identifier: PA2826421199
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile21750Thr
CA237836
NM_001256850.1:c.65249T>C