Canonical Allele Identifier: PA2830204472
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466750
ClinVar RCV Id: RCV000547265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp32828Glu
CA349406705
NM_133378.4:c.98484T>G
CA349406709
NM_133378.4:c.98484T>A