Canonical Allele Identifier: PA2830217970
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg13056Cys
CA1991600
NM_133432.3:c.39166C>T