Canonical Allele Identifier: PA2826415781
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val11637Ile
CA181830
NM_001256850.1:c.34909G>A