Canonical Allele Identifier: PA312123
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser9237Ala
CA312121
NM_001267550.2:c.27709T>G