Canonical Allele Identifier: PA658666005
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val18971Met
CA1993160
NM_001267550.2:c.56911G>A