Canonical Allele Identifier: PA2830221889
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr19553Ala
CA60984661
NM_133432.3:c.58657A>G