Canonical Allele Identifier: PA2830222847
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val21043Met
CA141176
NM_133432.3:c.63127G>A