Canonical Allele Identifier: PA2826412021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu3828Ala
CA2002711
NM_001256850.1:c.11483A>C