Canonical Allele Identifier: PA237838
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile23391Thr
CA237836
NM_001267550.2:c.70172T>C