Canonical Allele Identifier: PA2830202331
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile29435Thr
CA1986840
NM_133378.4:c.88304T>C