Canonical Allele Identifier: PA310396
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg23388Gln
CA310394
NM_001267550.2:c.70163G>A