Canonical Allele Identifier: PA2830215909
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser9512Pro
CA302469
NM_133432.3:c.28534T>C