Canonical Allele Identifier: PA2830190638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg740Ser
CA2005875
NM_133378.4:c.2218C>A