Canonical Allele Identifier: PA2830217381
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Lys12099Thr
CA10587487
NM_133432.3:c.36296A>C