Canonical Allele Identifier: PA916066332
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg8146Cys
CA1994260
NM_133437.4:c.24436C>T