Canonical Allele Identifier: PA2830216499
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202736
ClinVar RCV Id: RCV000184656
ClinVar Variation Id: 467313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp10550Glu
CA310128
NM_133432.3:c.31650T>G
CA1992846
NM_133432.3:c.31650T>A