Canonical Allele Identifier: PA2830224891
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met24016Val
CA178391
NM_133432.3:c.72046A>G