Canonical Allele Identifier: PA645382456
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ser867Gly
CA2005779
NM_133379.5:c.2599A>G