Canonical Allele Identifier: PA2826412284
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr4351Ala
CA2002496
NM_001256850.1:c.13051A>G