Canonical Allele Identifier: PA916064569
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg4628His
CA178865
NM_133437.4:c.13883G>A