Canonical Allele Identifier: PA2830216437
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr10457Met
CA178656
NM_133432.3:c.31370C>T