Canonical Allele Identifier: PA2830209815
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser403Thr
CA185027
NM_133432.3:c.1208G>C