Canonical Allele Identifier: PA2830204000
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2021831
ClinVar RCV Id: RCV002847316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32237Gly
CA349411785
NM_133378.4:c.96709C>G