Canonical Allele Identifier: PA2830224798
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp23882Gly
CA178394
NM_133432.3:c.71645A>G