Canonical Allele Identifier: PA2829431877
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr4305Ala
CA2002496
NM_003319.4:c.12913A>G