Canonical Allele Identifier: PA311027
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile32482Thr
CA311025
NM_001267550.2:c.97445T>C