Canonical Allele Identifier: PA916064513
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gln547Arg
CA2006003
NM_133437.4:c.1640A>G