Canonical Allele Identifier: PA2830222239
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met20106Arg
CA181669
NM_133432.3:c.60317T>G