Canonical Allele Identifier: PA2830199308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala22519Thr
CA1990080
NM_133378.4:c.67555G>A