Canonical Allele Identifier: PA658806522
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Glu2272Asp
CA349681831
NM_133379.5:c.6816A>T
CA349681833
NM_133379.5:c.6816A>C