Canonical Allele Identifier: PA2830227149
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2946668
ClinVar RCV Id: RCV003808906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu26424Asp
CA349407049
NM_133432.3:c.79272A>T
CA349407050
NM_133432.3:c.79272A>C