Canonical Allele Identifier: PA2830216281
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met10188Val
CA1993056
NM_133432.3:c.30562A>G