Canonical Allele Identifier: PA2830238979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly20789Ser
CA181649
NM_133437.4:c.62365G>A