Canonical Allele Identifier: PA311262
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Pro1207Thr
CA311258
NM_133379.5:c.3619C>A