Canonical Allele Identifier: PA2826418726
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 500219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly17311Val
CA1993173
NM_001256850.1:c.51932G>T