Canonical Allele Identifier: PA916065859
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg7182His
CA309911
NM_133437.4:c.21545G>A