Canonical Allele Identifier: PA645410797
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg23084Gln
CA1990959
NM_001267550.2:c.69251G>A