Canonical Allele Identifier: PA916065752
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 451886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu7027Lys
CA1995003
NM_133437.4:c.21079G>A