Canonical Allele Identifier: PA2830196221
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Phe15186Ser
CA1993835
NM_133378.4:c.45557T>C