Canonical Allele Identifier: PA2829445565
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 177968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser26006Cys
CA181087
NM_003319.4:c.78017C>G