Canonical Allele Identifier: PA310151
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val19886Gly
CA310149
NM_001267550.2:c.59657T>G