Canonical Allele Identifier: PA658816859
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile32003Thr
CA1986840
NM_001267550.2:c.96008T>C