Canonical Allele Identifier: PA2830210554
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu1128Asp
CA2005539
NM_133432.3:c.3384A>C
CA349483110
NM_133432.3:c.3384A>T