Canonical Allele Identifier: PA2829440605
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr19428Ala
CA60984661
NM_003319.4:c.58282A>G