Canonical Allele Identifier: PA2826489296
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg740Ser
CA2005875
NM_001267550.2:c.2218C>A