Canonical Allele Identifier: PA2830226260
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Lys25620Arg
CA311157
NM_133432.3:c.76859A>G