Canonical Allele Identifier: PA311261
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro1207Thr
CA311258
NM_001267550.2:c.3619C>A