Canonical Allele Identifier: PA916064425
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 208947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val351Met
CA210245
NM_133437.4:c.1051G>A