Canonical Allele Identifier: PA645409821
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe14840Tyr
CA10611673
NM_001267550.2:c.44519T>A