Canonical Allele Identifier: PA2829436489
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_003310.4:p.Gly12623Arg
CA1991786
NM_003319.4:c.37867G>C
CA1991787
NM_003319.4:c.37867G>A