Canonical Allele Identifier: PA2830227690
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val26988Glu
CA1984876
NM_133432.3:c.80963T>A