Canonical Allele Identifier: PA2830226904
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg26196Trp
CA1985267
NM_133432.3:c.78586C>T