Canonical Allele Identifier: PA916061049
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu9430Pro
CA1998764
NM_133378.4:c.28289T>C