Canonical Allele Identifier: PA2829431594
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu3782Ala
CA2002711
NM_003319.4:c.11345A>C