Canonical Allele Identifier: PA2830226557
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1034511
ClinVar RCV Id: RCV001337245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val25869Leu
CA1985429
NM_133432.3:c.77605G>C
CA349411760
NM_133432.3:c.77605G>T