Canonical Allele Identifier: PA2830208917
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr31825Pro
CA60957488
NM_133378.4:c.95473A>C