Canonical Allele Identifier: PA2830232500
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 500219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly10079Val
CA1993173
NM_133437.4:c.30236G>T