Canonical Allele Identifier: PA2499243558
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_001254479.2:p.Gly21688Arg
CA1991786
NM_001267550.2:c.65062G>C
CA1991787
NM_001267550.2:c.65062G>A