Canonical Allele Identifier: PA302915
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly27921Asp
CA302913
NM_001256850.1:c.83762G>A