Canonical Allele Identifier: PA2830197834
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_596869.4:p.Gly19120Arg
CA1991786
NM_133378.4:c.57358G>C
CA1991787
NM_133378.4:c.57358G>A