Canonical Allele Identifier: PA2829445097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile25602Thr
CA183120
NM_003319.4:c.76805T>C