Canonical Allele Identifier: PA645382332
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Gly736Arg
CA10576581
NM_133379.5:c.2206G>A
CA349501068
NM_133379.5:c.2206G>C