Canonical Allele Identifier: PA645409931
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg15898Gln
CA1995005
NM_001267550.2:c.47693G>A