Canonical Allele Identifier: PA2826427780
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val32533Ile
CA181577
NM_001256850.1:c.97597G>A