Canonical Allele Identifier: PA302472
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser18452Pro
CA302469
NM_001267550.2:c.55354T>C