Canonical Allele Identifier: PA2830216721
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val10946Gly
CA310149
NM_133432.3:c.32837T>G