Canonical Allele Identifier: PA2830205155
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 208947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val351Met
CA210245
NM_133378.4:c.1051G>A