Canonical Allele Identifier: PA2826492859
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr1891Cys
CA2005148
NM_001267550.2:c.5672A>G