Canonical Allele Identifier: PA2830216531
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu10606Gln
CA283500
NM_133432.3:c.31816G>C