Canonical Allele Identifier: PA916065213
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg5864His
CA1995719
NM_133437.4:c.17591G>A