Canonical Allele Identifier: PA2830243227
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_597681.4:p.Ala26255Val
CA1985269
NM_133437.4:c.78764C>T
CA2580064928
NM_133437.4:c.78764_78765delinsTG