Canonical Allele Identifier: PA2830202657
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp30139His
CA349434738
NM_133378.4:c.90415G>C