Canonical Allele Identifier: PA645409469
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile10271Val
CA1999029
NM_001267550.2:c.30811A>G