Canonical Allele Identifier: PA2830209716
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val307Met
CA2006172
NM_133432.3:c.919G>A