Canonical Allele Identifier: PA341211
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu33388Pro
CA341209
NM_133378.4:c.100163T>C