Canonical Allele Identifier: PA2830213876
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Lys5868Thr
CA1995649
NM_133432.3:c.17603A>C