Canonical Allele Identifier: PA2830227137
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238698
ClinVar RCV Id: RCV000232973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gln26414Arg
CA1985167
NM_133432.3:c.79241A>G