Canonical Allele Identifier: PA2830191901
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala3602Thr
CA2002382
NM_133378.4:c.10804G>A