Canonical Allele Identifier: PA302730
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 193962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val10286Ile
CA302729
NM_001256850.1:c.30856G>A