Canonical Allele Identifier: PA2830229221
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala1384Glu
CA311349
NM_133437.4:c.4151C>A