Canonical Allele Identifier: PA2830212813
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu3907Ala
CA2002711
NM_133432.3:c.11720A>C