Canonical Allele Identifier: PA2830219487
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg15495Cys
CA310469
NM_133432.3:c.46483C>T