Canonical Allele Identifier: PA2829445866
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2946668
ClinVar RCV Id: RCV003808906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu26299Asp
CA349407049
NM_003319.4:c.78897A>T
CA349407050
NM_003319.4:c.78897A>C