Canonical Allele Identifier: PA310214
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20908Gln
CA310212
NM_001267550.2:c.62723G>A