Canonical Allele Identifier: PA2830198835
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile21392Thr
CA1990576
NM_133378.4:c.64175T>C