Canonical Allele Identifier: PA658816500
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser29253Asn
CA1988262
NM_001267550.2:c.87758G>A