Canonical Allele Identifier: PA645411429
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro27673Thr
CA1988986
NM_001267550.2:c.83017C>A