Canonical Allele Identifier: PA2830243365
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 262342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala26373Gly
CA1985217
NM_133437.4:c.79118C>G