Canonical Allele Identifier: PA2826423289
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile25514Thr
CA140878
NM_001256850.1:c.76541T>C