Canonical Allele Identifier: PA181571
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32069Gln
CA181570
NM_133378.4:c.96206G>A