Canonical Allele Identifier: PA2830238861
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg20632His
CA1988138
NM_133437.4:c.61895G>A