Canonical Allele Identifier: PA2826413113
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val6029Met
CA2001483
NM_001256850.1:c.18085G>A