Canonical Allele Identifier: PA302631
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly12425Glu
CA302630
NM_133378.4:c.37274G>A