Canonical Allele Identifier: PA2830229003
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val1053Met
CA139572
NM_133437.4:c.3157G>A