Canonical Allele Identifier: PA2830205525
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val20981Ile
CA1990755
NM_133378.4:c.62941G>A