Canonical Allele Identifier: PA2829431650
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val3887Met
CA181936
NM_003319.4:c.11659G>A