Canonical Allele Identifier: PA2830216171
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 500219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly10012Val
CA1993173
NM_133432.3:c.30035G>T