Canonical Allele Identifier: PA645410280
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr18845Pro
CA1993236
NM_001267550.2:c.56533A>C