Canonical Allele Identifier: PA310130
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_001254479.2:p.Asp19490Glu
CA310128
NM_001267550.2:c.58470T>G
CA1992846
NM_001267550.2:c.58470T>A