Canonical Allele Identifier: PA2830233712
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Lys12166Thr
CA10587487
NM_133437.4:c.36497A>C