Canonical Allele Identifier: PA2830190635
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly736Arg
CA10576581
NM_133378.4:c.2206G>A
CA349501068
NM_133378.4:c.2206G>C