Canonical Allele Identifier: PA916065997
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg7355His
CA309929
NM_133437.4:c.22064G>A