Canonical Allele Identifier: PA2830226896
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332687
ClinVar Variation Id: 1760755
ClinVar RCV Id: RCV002409974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala26188Val
CA1985269
NM_133432.3:c.78563C>T
CA2580064928
NM_133432.3:c.78563_78564delinsTG