Canonical Allele Identifier: PA183316
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile35609Met
CA183314
NM_001267550.2:c.106827T>G