Canonical Allele Identifier: PA2826491756
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser867Gly
CA2005779
NM_001267550.2:c.2599A>G