Canonical Allele Identifier: PA916065371
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg6094Gln
CA309829
NM_133437.4:c.18281G>A