Canonical Allele Identifier: PA2829430866
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr2499Ile
CA61006134
NM_003319.4:c.7496C>T