Canonical Allele Identifier: PA645409370
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr9239His
CA1999737
NM_001267550.2:c.27715T>C