Canonical Allele Identifier: PA645411639
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28491His
CA1988633
NM_001267550.2:c.85472G>A