Canonical Allele Identifier: PA2829443289
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile23417Thr
CA311025
NM_003319.4:c.70250T>C