Canonical Allele Identifier: PA2830214302
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.His6703Arg
CA181794
NM_133432.3:c.20108A>G