Canonical Allele Identifier: PA231601
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly17182Ser
CA231599
NM_133378.4:c.51544G>A