Canonical Allele Identifier: PA2830219976
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg16404Trp
CA1989963
NM_133432.3:c.49210C>T