Canonical Allele Identifier: PA2830222646
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly20722Ser
CA181649
NM_133432.3:c.62164G>A