Canonical Allele Identifier: PA2830217773
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1034245
ClinVar RCV Id: RCV001336916
ClinVar Variation Id: 1254129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly12748Arg
CA1991786
NM_133432.3:c.38242G>C
CA1991787
NM_133432.3:c.38242G>A