Canonical Allele Identifier: PA2830214411
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile6899Thr
CA309893
NM_133432.3:c.20696T>C