Canonical Allele Identifier: PA2830222499
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr20507Arg
CA181662
NM_133432.3:c.61520C>G