Canonical Allele Identifier: PA2830209767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 208947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val351Met
CA210245
NM_133432.3:c.1051G>A