Canonical Allele Identifier: PA2830228767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala697Thr
CA346741
NM_133437.4:c.2089G>A